Canonical Allele Identifier: CA413716600
Gene: PGK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.77378767G>C (hg19) chrX:g.78123270G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.78123270G>C , CM000685.2:g.78123270G>C GRCh38
NC_000023.10:g.77378767G>C , CM000685.1:g.77378767G>C GRCh37
NC_000023.9:g.77265423G>C NCBI36
NG_008862.1:g.24102G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373316.5:c.832G>C MANE Select ENSP00000362413.4:p.Val278Leu
ENST00000644362.1:c.748G>C ENSP00000496140.1:p.Val250Leu
ENST00000373316.4:c.832G>C ENSP00000362413.4:p.Val278Leu
ENST00000474281.1:n.239G>C
NM_000291.3:c.832G>C NP_000282.1:p.Val278Leu
NM_000291.4:c.832G>C MANE Select NP_000282.1:p.Val278Leu
Search 100 bp 5'
Search 100 bp 3'